ENST00000472571.2 VCF2

Information
Transcript ID
ENST00000472571.2
Genome
hg38
Position
chrX:55,145,356-55,161,182
Strand
-
CDS length
141
Amino acid length
47
Gene symbol
VCF2
Gene type
protein-coding
Gene description
VCP nuclear cofactor family member 2
Gene Entrez Gene ID
90736
Variants

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Target data :
MGeND data only
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
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Target data :
MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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Target data :
MGeND data only
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Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Exon
Exon number Start Stop
3 55,145,356 55,146,311
2 55,159,122 55,159,228
1 55,161,137 55,161,182
CDS
Exon number Type Start Stop
3 CDS 55,146,298 55,146,311
2 CDS 55,159,122 55,159,228
1 CDS 55,161,137 55,161,156
Other genome
Genome Chromosome Start End Links
hg19 chrX 55,171,789 55,187,615 Link
CDS sequence
ATGGGAGGCTGCCCTGTACGGAAAAGAAGAAGAAATGGCAGTAAAGAGGGCAACCATCATTCCACCCAGCCCAAAAGGAATAAGAGAAACCCTATCTTTCAGGATTCTCAAGATACAGAGGTAGCAATTTTCATGGAGTGA
Amino sequence
MGGCPVRKRRRNGSKEGNHHSTQPKRNKRNPIFQDSQDTEVAIFME*